nsv4449033
- Organism: Homo sapiens
- Study:nstd175 (Genome in a Bottle)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:13,261
- Description:SVTYPE=DEL;REPTYPE=SIMPLEDEL
- Publication(s):Genome in a Bottle
Source: NCBI
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 936 SVs from 79 studies. See in: genome view
Overlapping variant regions from other studies: 936 SVs from 79 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv4449033 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000016.10 | Chr16 | 78,337,741 | 78,351,001 |
nsv4449033 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000016.9 | Chr16 | 78,371,638 | 78,384,898 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv15755836 | deletion | Sequencing | Sequence alignment |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv15755836 | Remapped | Perfect | NC_000016.10:g.783 37741_78351001del | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 78,337,741 | 78,351,001 |
nssv15755836 | Submitted genomic | NC_000016.9:g.7837 1638_78384898del | GRCh37 (hg19) | NC_000016.9 | Chr16 | 78,371,638 | 78,384,898 |